Hereditary angioedema with normal C1 inhibitor associated with carboxypeptidase N deficiency-Reference-Cited by-同舟云学术

Hereditary angioedema with normal C1 inhibitor associated with carboxypeptidase N deficiency

Published:2024-05 Issue:2 Volume:3 Page:100223
ISSN:2772-8293
Container-title:Journal of Allergy and Clinical Immunology: Global
language:en
Short-container-title:Journal of Allergy and Clinical Immunology: Global

Author:

Vincent Denis,Parsopoulou Faidra,Martin Ludovic,Gaboriaud Christine,Demongeot Jacques,Loules Gedeon,Fischer Sascha,Cichon Sven,Germenis Anastasios E.,Ghannam Arije,Drouet Christian^ORCID

Funder

Agence nationale de la recherche

Publisher

Elsevier BV

Reference51 articles.

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2. Misdiagnosis trends in patients with hereditary angioedema from the real-world clinical setting;Zanichelli;Ann Allergy Asthma Immunol,2016

3. Missense mutations in the coagulation factor XII (Hageman factor) gene in hereditary angioedema with normal C1 inhibitor;Dewald;Biochem Biophys Res Commun,2006

4. Increased activity of coagulation factor XII (Hageman factor) causes hereditary angioedema type III;Cichon;Am J Hum Genet,2006

5. Hereditary angioedema with a mutation in the plasminogen gene;Bork;Allergy,2018

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1. Analysis of disease burden in patients with hereditary angioedema from Japan by patient‐reported outcomes;The Journal of Dermatology;2024-09-11

2. Hereditary angioedema classification: Expanding knowledge by genotyping and endotyping;World Allergy Organization Journal;2024-05